Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 1
rs6987702 8 125492484 intron variant T/C snv 0.43 1
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 1
rs7616006 3 12226148 intergenic variant A/G snv 0.48 1
rs8106503 19 11086210 upstream gene variant T/C snv 0.16 1
rs8180991 8 125488108 intron variant C/G snv 0.19 1
rs10115928
ABCA1
9 104888562 intron variant C/T snv 0.47 1
rs2575875
ABCA1
9 104900213 intron variant G/A snv 0.46 1
rs2777784
ABCA1
9 104898778 intron variant A/G snv 0.47 1
rs2287623
ABCB11
2 168973645 intron variant G/A snv 0.57 1
rs16967179
ABCC1
16 15997650 intron variant C/T snv 2.0E-02 1
rs8056298
ABCC1
16 16142666 3 prime UTR variant T/G snv 0.95 1
rs4148613
ABCC8
0.925 0.120 11 17454913 intron variant C/G snv 4.8E-03 1
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv 1
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 1
rs6739874
ACADL
2 210196946 intron variant G/T snv 1.7E-02 1
rs8026235
ACAN
15 88806225 intron variant A/C snv 1.7E-02 1
rs35025137
ADAM12
10 126101214 missense variant C/T snv 5.6E-05 4.9E-05 1
rs13329672
ALDH1A2
15 58407738 intron variant C/T snv 0.31 1
rs1601935
ALDH1A2
15 58379566 intron variant G/T snv 0.60 1
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32 1
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 1
rs7350789
ALDH1A2
15 58387469 intron variant G/A snv 0.35 1
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 1
rs769446
APOE
0.882 0.120 19 44905371 upstream gene variant T/C snv 7.0E-02 1